Variants in gene NIN with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 7

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HGVS	dbSNP	gnomAD frequency
NM_020921.4(NIN):c.3197T>A (p.Val1066Asp)	rs78280523	0.00316
NM_020921.4(NIN):c.2987C>T (p.Ala996Val)	rs41313507	0.00235
NM_020921.4(NIN):c.2665G>C (p.Val889Leu)	rs78251482	0.00231
NM_020921.4(NIN):c.3080CTC[1] (p.Pro1028del)	rs369382014
NM_020921.4(NIN):c.5323G>A (p.Val1775Met)	rs375323558
NM_020921.4(NIN):c.5877+3A>G
NM_020921.4(NIN):c.673G>A (p.Glu225Lys)

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